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阿片类物质对神经元放电的抑制作用:反对环核苷酸参与其中的证据。

Inhibition of neuronal firing by opiates: evidence against the involvement of cyclic nucleotides.

作者信息

Karras P J, North R A

出版信息

Br J Pharmacol. 1979 Apr;65(4):647-52. doi: 10.1111/j.1476-5381.1979.tb07877.x.

Abstract
  1. Extracellular recordings were made in vitro from single neurones of the myenteric plexus of the guinea-pig ileum. 2. Neuronal firing was inhibited by morphine and normorphine (10 nM to 1 micrometer). Cyclic adenosine 3',5'-monophosphate (cyclic AMP) (100 micrometer to 1 mM) also inhibited the firing of the majority of the neurones. Prostaglandin E2 usually caused a short-lasting excitation of myenteric neurones and the phosphodiesterase inhibitor 3-isobutyl-1-methylxanthine was usually without effect on firing rate. 3. The inhibition of neuronal firing by normorphine was unaffected by prior and/or concurrent administration of cyclic AMP, dibutyryl cyclic adenosine 3',5'-monophosphate, prostaglandin E2 or 3-isobutyl-1-methylxanthine. As these four treatments might be expected to elevate intracellular levels of cyclic AMP, the results lend no support to the notion that a reduction in intracellular cyclic AMP is essential to the inhibition of firing produced by morphine.
摘要
  1. 在体外对豚鼠回肠肌间神经丛的单个神经元进行细胞外记录。2. 吗啡和去甲吗啡(10 nM至1微米)可抑制神经元放电。环磷酸腺苷(cAMP)(100微米至1 mM)也能抑制大多数神经元的放电。前列腺素E2通常会引起肌间神经元短暂兴奋,而磷酸二酯酶抑制剂3 - 异丁基 - 1 - 甲基黄嘌呤通常对放电频率无影响。3. 去甲吗啡对神经元放电的抑制作用不受预先和/或同时给予cAMP、二丁酰环磷酸腺苷、前列腺素E2或3 - 异丁基 - 1 - 甲基黄嘌呤的影响。由于这四种处理预期会提高细胞内cAMP水平,这些结果不支持细胞内cAMP减少对吗啡产生的放电抑制至关重要这一观点。

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Kinetic parameters of narcotic agonists and antagonists, with particular reference to N-allylnoroxymorphone (naloxone).
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6
The action of norepinephrine in the rat hippocampus. I. Iontophoretic studies.
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